IRBESARTAN

NDC 42658-122 · Hisun Pharmaceuticals USA Inc.

Generic nameIRBESARTAN

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)IRBESARTAN

Strength150 mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]

Marketing categoryANDA

Packages

42658-122-01 — 30 TABLET, FILM COATED in 1 BOTTLE (42658-122-01)

42658-122-04 — 90 TABLET, FILM COATED in 1 BOTTLE (42658-122-04)

42658-122-07 — 500 TABLET, FILM COATED in 1 BOTTLE (42658-122-07)

FDA lists these products with the same active ingredient.

31722-731 — Irbesartan, 33342-047 — Irbesartan, 33342-048 — Irbesartan, 33342-049 — Irbesartan, 33342-057 — Irbesartan and Hydrochlorothiazide, 33342-058 — Irbesartan and Hydrochlorothiazide, 42291-940 — IRBESARTAN, 42291-941 — IRBESARTAN, 42291-942 — IRBESARTAN, 42658-121 — IRBESARTAN, 42658-123 — IRBESARTAN, 43547-330 — Irbesartan and Hydrochlorothiazide, 43547-331 — Irbesartan and Hydrochlorothiazide, 43547-374 — Irbesartan, 43547-375 — Irbesartan, 43547-376 — Irbesartan, 46708-439 — IRBESARTAN, 46708-440 — IRBESARTAN, 46708-441 — IRBESARTAN, 46708-442 — Irbesartan and Hydrochlorothiazide, +95 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.